Publication: Grebe Syndrome - Case Report With Review of Literature
| creativeworkseries.issn | ISSN 1990-7974 eISSN 1990-7982 | |
| dc.contributor.author | Nagaraj, Rashmi | |
| dc.contributor.author | Kiran, HS | |
| dc.date.accessioned | 2025-11-30T08:56:44Z | |
| dc.date.available | 2025-11-30T08:56:44Z | |
| dc.date.issued | 2021 | |
| dc.description | Rashmi Nagaraj Department of Paediatrics, JSS Medical College, JSSAHER, Mysore, India HS Kiran Department of Internal medicine, JSS Medical College, JSSAHER, Mysore, India | |
| dc.description.abstract | Abstract Grebe syndrome is a rare genetic condition characterized by short limb dwarfism. It is transmitted by autosomal mode of inheritance. There are no associated anomalies and the affected child has normal intelligence and normal life span. This syndrome has a very low incidence and needs to be differentiated from other forms of short limb dwarfism since treatment options may vary. We have described here a severely affected case of the same with review of literature. | |
| dc.identifier | https://doi.org/10.3126/jnps.v41i3.31170 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/3307 | |
| dc.language.iso | en_US | |
| dc.publisher | Nepal Paediatric Society (JNPS) | |
| dc.subject | Acromesomelic shortening | |
| dc.subject | Chondrodysplasia | |
| dc.subject | Grebe syndrome | |
| dc.subject | Short limb dwarfism | |
| dc.title | Grebe Syndrome - Case Report With Review of Literature | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 450 | |
| oaire.citation.startPage | 447 | |
| relation.isJournalIssueOfPublication | 0b99c152-1968-4a9d-81aa-91bd247df181 | |
| relation.isJournalIssueOfPublication.latestForDiscovery | 0b99c152-1968-4a9d-81aa-91bd247df181 | |
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